Clinical Research Study Finder

Children's Hospital of Philadelphia leads or participates in hundreds of clinical research studies and clinical trials. Many of the studies that are currently enrolling patients can be found in this database. Use this finder to learn more about the purpose of these studies and clinical trials, find out who can participate, and tell us you're interested in enrolling. You can also look for studies that offer remote participation from home!

Find a Clinical Research Study

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DoSES

This research is studying a vaccine against Mpox (formerly known as monkeypox) that is FDA approved for adults but not yet approved for children. The goal of the study is to determine if the vaccine protects children just as well as it protects adults. The study is also looking at the safety of the vaccine. This study is open to healthy adolescents, ages 12-17. In addition, adolescents with certain immunodeficiency diseases or other conditions, that are well controlled, are eligible to participate. 

18F-DOPA PET/CT scan for Hyperinsulinism

The purpose of this research is to study 18F-L-Fluoro-DOPA (F-DOPA), a tracer, which is used to take pictures of the pancreas. This imaging test is called an F-DOPA PET scan. The F-DOPA tracer is used to highlight areas of the pancreas that make too much insulin on the PET scan images. The test includes a CT scan (computerized tomography) done at the same time on the same machine, to help define exactly where the highlighted area is located within the pancreas and determine the location of blood vessels and other vital structures. 

Leigh Syndrome Natural History Study

The Children’s Hospital of Philadelphia is conducting a Natural History Study in Leigh Syndrome.

 

Natural History Studies help researchers better understand disease and can support drug development.


You or your child may qualify for this study if you have been diagnosed with Leigh Syndrome and are between the ages of 0 and 75. 

PRoMPT BOLUS

PRoMPT BOLUS will determine which of two commonly used IV fluid types is most effective to treat children with sepsis. Patients with possible septic shock will be treated with one of two types of IV fluid, both of which are part of standard of care--0.9% saline or balanced fluids (including lactated Ringer’s solution or Plasma-Lyte)--along with the best locally available medical care available for their symptoms. Because sepsis is an emergency, patients may be enrolled with “exception from informed consent” unless they opt-out. However, subjects/families will decide if their data can be used in the study. We are not aware of any reason, at this time, why anyone with sepsis would not choose to participate if awake and able to take part in decisions about their care.

IAMFIT

Researchers at CHOP are recruiting patients diagnosed with either acute leukemia (myeloid, lymphoid), myelodysplastic syndromes, or aplastic anemia and treated with allogeneic hematopoietic cell transplantation (HCT) within the past 6-48 months.


Research has shown that adolescents and young adults who are treated with HCT are at increased risk for skeletal muscle loss. So, the purpose of this study is to investigate if a combination of exercise training and an exercise supplement can mitigate this effect. The
supplement is called nicotinamide riboside.

Participants will be randomly assigned to 1 of 4 groups:
  • Exercise + Supplement
  • Exercise + Placebo
  • No Exercise + Supplement
  • No Exercise + Placebo
The study will provide all the exercise equipment required to complete the exercise intervention, including remote sessions.

Body Surface Gastric Mapping in Patients with GI Symptoms

The purpose of this study is to learn more about a new device that measures stomach myoelectric (electricity produced by muscles) activity in children and young adults using body surface gastric mapping (BSGM). The BSGM device is FDA approved in adults but not children under 18. 

We are looking to partner with patients who have a confirmed diagnosis of a Motility Disorder and/or Functional Gastrointestinal Disorder (FGID) or patients who are having motility tests/procedures performed for clinical care. We are also looking for healthy controls without any history of inflammatory disease or pyloric disorders. All study participants must be 8 - 25 years of age and have a body mass index (BMI) of less than 35. 

Participation is completely voluntary, and subjects may withdraw at any time without affecting their care. Participants may receive compensation for their time.

MPS Biomarkers of Joint Disease

The purpose of this study is to establish connections between biomarkers (a measurable substance in your blood, urine, or saliva) and the stage and grade of bone and cartilage disease in MPS patients. 

Neurocognition in Hyperinsulinism

The purpose of this study is to understand how cognitive function changes over time in children with hyperinsulinism (HI) compared to children who are healthy volunteers. Participants will be asked to complete cognitive function tasks and questionnaires three times over the course of two years: at the start of the study, one year later, and one year after that. Each visit is approximately 2 hours. If you like, you can receive a summary of the results from the tasks. Compensation is provided for your time and effort. 

OT-58 for Homocystinuria

This research study is focused on patients who have Cystathionine beta synthase deficiency Homocystinuria (CBSDH). The purpose of this study is to test the safety and tolerability of an investigational drug called OT-58 (the study drug). An “investigational drug” is a drug that is being tested and is not approved by the U.S. Food and Drug Administration (FDA). Specifically, this study will measure how much OT-58 gets into the blood stream, how long it takes the body to get rid of it, and whether it reduces the amount of homocysteine in your blood. 

ML-004 for Adolescents and Adults With ASD

The purpose of this study is to test the safety of an investigational medicine called ML-004 and how it might affect communication, behavior, and other symptoms of autism spectrum disorder (ASD).  This medication is investigational because it has not been approved by the FDA for the treatment of symptoms associated with autism. 
You may qualify if you: 
  • Are 12 to 25 years old
  • Have an autism diagnosis
  • Have a designated care/study partner able to attend every visit and answer questions about the participant. This person does not need to be the participant's parent or guardian. This person should have significant contact with them and can support them for the duration of the study. 
  • Are able to swallow the study medication (tablet)


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